Thrombosis Research Group EA 3065, University Jean Monnet, Saint-Etienne, France.
Thromb Haemost. 2010 Aug;104(2):252-60. doi: 10.1160/TH10-02-0127. Epub 2010 Jun 10.
Fondaparinux is a synthetic antithrombotic agent with specific anti-factor Xa activity. A population pharmacokinetic model of fondaparinux, based on data obtained in patients included in phase II/III trials, has been described. However, the validity of this model in everyday practice needed to be confirmed. This study was a multicenter, prospective cohort study in consecutive orthopaedic patients treated with 2.5 mg of fondaparinux. Anti-Xa activities were recorded in 809 patients. Population parameters and inter-individual variability were estimated using NONMEM VI software. A two-compartment model with first-order absorption best described fondaparinux pharmacokinetics. Covariates partly explaining inter-individual variability were body weight, age and creatinine clearance estimated by the simplified Modification of Diet in Renal Disease formula (MDRD). A body weight less than 50 kg and moderate renal failure increased drug exposure. Although the population pharmacokinetic model of fondaparinux was described, this one requires to be validated in everyday practice.
磺达肝癸钠是一种具有特定抗因子 Xa 活性的合成抗血栓药物。磺达肝癸钠的群体药代动力学模型是基于 II/III 期临床试验中纳入的患者数据建立的。然而,该模型在日常实践中的有效性需要得到证实。本研究是一项多中心、前瞻性队列研究,连续纳入接受 2.5mg 磺达肝癸钠治疗的骨科患者。在 809 例患者中记录了抗-Xa 活性。使用 NONMEM VI 软件估计群体参数和个体间变异性。具有一级吸收的两室模型最能描述磺达肝癸钠的药代动力学。部分解释个体间变异性的协变量为体重、年龄和简化肾脏病饮食改良公式(MDRD)估计的肌酐清除率。体重低于 50kg 和中度肾功能衰竭会增加药物暴露。尽管已经描述了磺达肝癸钠的群体药代动力学模型,但该模型在日常实践中仍需要验证。